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2 型糖尿病中无机硝酸盐代谢作用的翻译缺失:抗坏血酸是答案吗?

Lost-in-Translation of Metabolic Effects of Inorganic Nitrate in Type 2 Diabetes: Is Ascorbic Acid the Answer?

机构信息

Nutrition and Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran 1985717413, Iran.

Department of Molecular, Cellular and Biomedical Sciences, Sophie Davis School of Biomedical Education, City University of New York School of Medicine, New York, NY 10031, USA.

出版信息

Int J Mol Sci. 2021 Apr 29;22(9):4735. doi: 10.3390/ijms22094735.

Abstract

Beneficial metabolic effects of inorganic nitrate (NO) and nitrite (NO) in type 2 diabetes mellitus (T2DM) have been documented in animal experiments; however, this is not the case for humans. Although it has remained an open question, the redox environment affecting the conversion of NO to NO and then to NO is suggested as a potential reason for this lost-in-translation. Ascorbic acid (AA) has a critical role in the gastric conversion of NO to NO following ingestion of NO. In contrast to AA-synthesizing species like rats, the lack of ability to synthesize AA and a lower AA body pool and plasma concentrations may partly explain why humans with T2DM do not benefit from NO/NO supplementation. Rats also have higher AA concentrations in their stomach tissue and gastric juice that can significantly potentiate gastric NO-to-NO conversion. Here, we hypothesized that the lack of beneficial metabolic effects of inorganic NO in patients with T2DM may be at least in part attributed to species differences in AA metabolism and also abnormal metabolism of AA in patients with T2DM. If this hypothesis is proved to be correct, then patients with T2DM may need supplementation of AA to attain the beneficial metabolic effects of inorganic NO therapy.

摘要

在动物实验中已经证实了无机硝酸盐(NO)和亚硝酸盐(NO)对 2 型糖尿病(T2DM)的有益代谢作用;然而,这在人类中并不适用。尽管这仍然是一个悬而未决的问题,但影响 NO 向 NO 再向 NO 转化的氧化还原环境被认为是这种转化缺失的一个潜在原因。抗坏血酸(AA)在摄入 NO 后胃内将 NO 转化为 NO 中起着关键作用。与能够合成 AA 的物种(如大鼠)不同,人类缺乏合成 AA 的能力,AA 体池和血浆浓度较低,这可能部分解释了为什么 T2DM 患者不能从 NO/NO 补充中获益。大鼠的胃组织和胃液中也含有更高浓度的 AA,这可以显著增强胃内 NO 向 NO 的转化。在这里,我们假设 T2DM 患者无机 NO 缺乏有益代谢作用的原因至少部分归因于 AA 代谢的物种差异,以及 T2DM 患者 AA 代谢的异常。如果这一假设被证明是正确的,那么 T2DM 患者可能需要补充 AA,以获得无机 NO 治疗的有益代谢作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f519/8124635/588b60e0a349/ijms-22-04735-g001.jpg

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